NUT rabbit pAb
Disease: A chromosomal aberration involving NUT is found in a rare, aggressive, and lethal carcinoma arising in midline organs of young people. Translocation t (15;19) (q14;p13) with BRD4 which produces a BRD4-NUT fusion protein. Disease: A chromosomal aberration involving NUT is found in a rare, aggressive, and lethal carcinoma arising in midline organs of young people. Translocation t (15;9) (q14;q34) with BRD3 which produces a BRD3-NUT fusion protein. PTM: Phosphorylation on Ser-1026, Ser-1029 or Ser-1031 is important for cytoplasmic export. similarity: Belongs to the FAM22 family. subcellular location: Shuttles between nucleus and cytoplasm. tissue specificity: Specifically expressed in testis.
Product Specifications
Background
Product Name Alternative
Protein NUT (Nuclear protein in testis)
UniProt
Q86Y26
Swiss Prot
Q86Y26
Reactivity
Human; Rat; Mouse
Immunogen
Synthesized peptide derived from human NUT. at AA range: 1082-1131
Target
NUT
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:500-2000, ELISA 1:10000-20000
Buffer
-20°C/1 year
Molecular Weight
63kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
63kD
Fragment
IgG
Subcellular Location
Cytoplasm . Nucleus . Shuttles between nucleus and cytoplasm. .
Other Product Names
Protein NUT (Nuclear protein in testis)
Gene ID (Human)
256646
Available Sizes
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